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Cycloalkenes, Allyl compounds

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Alkenes (3)
Cyclic compounds (3)
Drugs acting on the nervous system (3)
Psychoactive drugs (3)
Anticonvulsants (2)
Barbiturates (2)
Cyclohexenes (2)
Six-membered rings (2)
Analgesics (1)
Anesthetics (1)
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Cyclopentenes (1)
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Five-membered rings (1)
General anesthetics (1)
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Opioid antagonists (1)
Opioid receptor ligands (1)
Opioids (1)
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Semisynthetic opioids (1)
Thiobarbiturates (1)

Nalorphine (62-67-9)  
Allylnormorphine  ·  Nalorphine Hydrochloride  ·  Lethidrone
Nalorphine (INN) (brand names Lethidrone, Nalline), also known as N-allylnormorphine, is a mixed opioid agonist–antagonist with opioid antagonist and analgesic properties. It was introduced in 1954 and was used as an antidote to reverse opioid overdose and in a challenge test to determine opioid dependence. It acts at two opioid receptors — the μ-opioid receptor (MOR) where it has antagonistic effects, and at the κ-opioid receptor (KOR) (Ki = 1.6 nM; EC50 = 483 nM; Emax = 95%) where it exerts high-efficacy partial agonist/near-full agonist characteristics.
Cyclopentobarbital (76-68-6)  
Cyclopentobarbital sodium (Cyclopal, Dormisan) is a barbiturate derivative invented in the 1940s. It has sedative and anticonvulsant properties, and was used primarily as an anaesthetic in veterinary medicine. Cyclopal is considered similar in effects to phenobarbital but lasts almost three times as long, and is considered a long-acting barbiturate with a fairly slow onset of action.
Thialbarbital (467-36-7)  
Thialbarbital (Intranarcon) is a barbiturate derivative invented in the 1960s. It has sedative effects, and was used primarily for induction in surgical anaesthesia. Thialbarbital is short acting and has less of a tendency to induce respiratory depression than other barbiturate derivatives such as pentobarbital.
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Cycloalkenes
Allyl compounds